Canonical Allele Identifier: CA367637326

Gene: GUSB

Linked Data

• MyVariant Identifiers: chr7:g.65425979G>C (hg19) ; chr7:g.65960992G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.65960992G>C , CM000669.2:g.65960992G>C	GRCh38
NC_000007.13:g.65425979G>C , CM000669.1:g.65425979G>C	GRCh37
NC_000007.12:g.65063414G>C	NCBI36
NG_016197.1:g.26323C>G
NG_051954.1:g.92894G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304895.9:c.1861C>G MANE Select	ENSP00000302728.4:p.Leu621Val
ENST00000304895.8:c.1861C>G	ENSP00000302728.4:p.Leu621Val
ENST00000421103.5:c.1423C>G	ENSP00000391390.1:p.Leu475Val
ENST00000430730.5:c.*1128C>G	ENSP00000411859.1:n.*1128C>G
ENST00000447929.5:c.*1241C>G	ENSP00000411262.1:n.*1241C>G
ENST00000466883.5:n.2251C>G
NM_000181.3:c.1861C>G	NP_000172.2:p.Leu621Val
NM_001284290.1:c.1423C>G	NP_001271219.1:p.Leu475Val
NM_001293104.1:c.1291C>G	NP_001280033.1:p.Leu431Val
NM_001293105.1:c.1204C>G	NP_001280034.1:p.Leu402Val
NR_120531.1:n.1907C>G
XM_005250297.3:c.1708C>G	XP_005250354.1:p.Leu570Val
XM_011516113.1:c.1360C>G	XP_011514415.1:p.Leu454Val
XM_011516114.1:c.1189C>G	XP_011514416.1:p.Leu397Val
XM_005250297.4:c.1708C>G	XP_005250354.1:p.Leu570Val
XM_011516114.2:c.1189C>G	XP_011514416.1:p.Leu397Val
XM_017012091.1:c.1207C>G	XP_016867580.1:p.Leu403Val
XM_017012092.1:c.1138C>G	XP_016867581.1:p.Leu380Val
XM_017012093.2:c.1036C>G	XP_016867582.1:p.Leu346Val
XR_001744658.2:n.1668C>G
XR_001744659.2:n.1781C>G
XR_001744660.2:n.1713C>G
XR_001744661.2:n.1628C>G
XR_927461.3:n.1866C>G
NM_000181.4:c.1861C>G MANE Select	NP_000172.2:p.Leu621Val
NM_001284290.2:c.1423C>G	NP_001271219.1:p.Leu475Val
NM_001293104.2:c.1291C>G	NP_001280033.1:p.Leu431Val
NM_001293105.2:c.1204C>G	NP_001280034.1:p.Leu402Val
NR_120531.2:n.1806C>G